Thin film lamination delamination process to create very thin film on fabric

ABSTRACT

A process for transferring a thin polymeric film to either woven or non-woven fabrics by first coextruding the thin polymeric film with a plastic support layer, then adhesively laminating the polymeric film to a fabric, followed by delaminating the support layer. The thin base layer remaining on the fabric imparts desired properties to the fabric while maintaining the soft feel, or drapeability, of the fabric, as opposed to lamination of thicker polymeric films to fabrics.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The invention relates to the lamination and delamination of thin filmsto fabrics. More particularly, the invention pertains to a process forthe adhesion of thin films to either woven or non-woven fabrics for thepurpose of improving the drapeability of the fabrics as compared to thelamination of thicker films to fabrics.

2. Background of the Invention

Film to fabric laminations are well known techniques that are employedin order to impart certain properties of a polymeric film to a woven ornon-woven fabric. For example, it may be desirable to impart propertiessuch as opacity, controlled barrier or gas transport, moistureresistance or room darkness to a fabric, thus increasing the potentialapplications for which that fabric may be used. However, while it may bedesirable in certain applications for the film-fabric laminations tohave such improved properties as just mentioned, it is also importantthat the fabric retain a soft feel. For example, film to fabriclaminations are frequently used in forming surgical gowns havingimproved strength and a good moisture barrier, however the material mustalso feel soft so that it is comfortable to the person who is wearingit. Additionally, when forming other personal care products such asdiapers or surgical wraps, the soft feel of the material is of utmostimportance to the user. Film to fabric laminates are also used in otherapplications, such as textile applications, in which a soft drape is animportant factor to a consumer.

One problem associated with current film-fabric lamination techniques isthe unavoidable limitations on the thicknesses of the films to belaminated onto the fabrics. Specifically, known techniques require thatthick films (i.e. films having a thickness of at least 10 μm (0.40 mil))be laminated to the fabric. This is because of the processinglimitations of current coater and lamination equipment, specifically atthe very high tolerances of tension control required to laminate thinpolymer films to lightweight fabrics. However, films having a thicknessof 10 μm or greater are typically unable to retain the soft feel of thefabric. In addition, such thick film laminations are disadvantageousbecause they tend to reduce the flexibility of the fabric. Flexibilityof the fabric is often an important feature of a film-fabric lamination.

Therefore, there exists a need in the art to have a thin film-fabriclaminate film (i.e. a film-fabric laminate having a film thickness ofless than about 10 μm, preferably 8 μm or less) that can be economicallymanufactured and maintains the flexibility and soft feel of the fabricas compared to thicker film-fabric laminates.

SUMMARY OF THE INVENTION

The invention provides a thin film lamination-delamination processcomprising the steps of:

-   a) providing a plastic support layer having first and second    surfaces;-   b) applying at least one thin plastic base layer, having first and    second surfaces, onto at least one surface of said support layer,    with the first surface of said at least one thin base layer in    contact with a surface of said support layer;-   c) applying an adhesive layer onto the second surface of said second    base layer;-   d) attaching the base layer to a fabric via the adhesive layer; and-   e) separating the support layer from the base layer, such that the    base layer remains attached to the fabric.

The invention also provides a multilayered film comprising:

-   a) a plastic support layer having first and second surfaces;-   b) at least one thin plastic base layer, having first and second    surfaces, on at least one of said surfaces of said support layer,    with the first surface of said at least one thin base layer in    contact with a surface of said support layer;-   c) an adhesive layer on the second surface of said thin base layer;    and-   d) a fabric attached to said thin base layer via the adhesive layer.

The invention further provides a multilayered film comprising:

-   a) a fabric having a surface; and-   b) a thin plastic base layer attached to the surface of said fabric;    wherein said base layer has a thickness of from about 1 μm to about    10 μm, and wherein said thin base layer is adhesively attached to    the fabric.

The present invention overcomes the problems of the prior art byenabling a very thin film less than about 8 μm (0.32 mil) to belaminated to a woven or non-woven fabric. The invention enables a thinbase layer to be laminated to a fabric by first applying the thin baselayer onto a support or carrier layer and then transferring the thinfilm from the support layer to the fabric by laminating the supportlayer to the fabric via an intermediate adhesive layer, and thenstripping the support from the fabric, leaving the thin base layer onthe fabric.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The invention provides a thin film to fabric lamination-delaminationprocess in which a thin, self-supporting, polymeric base layer istransferred from a plastic support layer to a fabric. The support layerhas first and second surfaces and is coextruded with a polymericmaterial which forms a thin base layer having first and second surfaceswith the first surface of the base layer on the second surface of thesupport layer. An adhesive layer is then applied onto the second surfaceof the base layer. This structure is then laminated to a fabric receiversheet such that the adhesive layer is in contact with a surface of thefabric. After this lamination step, the fabric and support layer areseparated, leaving the base layer and adhesive layer on the fabric. Theresult is a material that is capable of producing articles having a softfeel.

The plastic support layer may comprise any suitable polymeric materialwhich has a thermal stability suitable for an adhesive laminationprocess. Suitable materials include polyolefins, polyamides, polyvinylchloride (PVC), ethylene vinyl acetate (EVA), polyesters, cyclo olefinpolymers and blends thereof. In the preferred embodiment of theinvention, the support layer comprises a polyamide.

Suitable polyamides (nylons) within the scope of the inventionnon-exclusively include homopolymers or copolymers selected fromaliphatic polyamides and aliphatic/aromatic polyamides having amolecular weight of from about 10,000 to about 100,000. Generalprocedures useful for the preparation of polyamides are well known tothe art, including the self-condensation of lactams and the reactionproducts of diacids with diamines.

Useful polyamide homopolymers include poly(4-aminobutyric acid) (nylon4), poly(6-aminohexanoic acid) (nylon 6, also known aspoly(caprolactam)), poly(7-aminoheptanoic acid) (nylon 7),poly(8-aminooctanoic acid)(nylon 8), poly(9-aminononanoic acid) (nylon9), poly(10-aminodecanoic acid) (nylon 10), poly(11-aminoundecanoicacid) (nylon 11), poly(12-aminododecanoic acid) (nylon 12), nylon 4,6,poly(hexamethylene adipamide) (nylon 6,6), poly(hexamethylenesebacamide) (nylon 6,10), poly(heptamethylene pimelamide) (nylon 7,7),poly(octamethylene suberamide) (nylon 8,8), poly(hexamethyleneazelamide) (nylon 6,9), poly(nonamethylene azelamide) (nylon 9,9),poly(decamethylene azelamide) (nylon 10,9),poly(tetramethylenediamine-co-oxalic acid) (nylon 4,2), the polyamide ofn-dodecanedioic acid and hexamethylenediamine (nylon 6,12), thepolyamide of dodecamethylenediamine and n-dodecanedioic acid (nylon12,12) and the like. Useful aliphatic polyamide copolymers includecaprolactam/hexamethylene adipamide copolymer (nylon 6,6/6),hexamethylene adipamide/caprolactam copolymer (nylon 6/6,6),trimethylene adipamide/hexamethylene azelaiamide copolymer (nylontrimethyl 6,2/6,2), hexamethylene adipamide-hexamethylene-azelaiamidecaprolactam copolymer (nylon 6,6/6,9/6) and the like. Also included areother nylons which are not particularly delineated here. Of thesepolyamides, preferred polyamides include nylon 6, nylon 6,6, nylon6/6,6, nylon 6,6/6 as well as mixtures of the same. The most preferredpolyamide is nylon 6.

Aliphatic polyamides used in the practice of this invention may beobtained from commercial sources or prepared in accordance with knownpreparatory techniques. For example, poly(caprolactam) can be obtainedfrom Honeywell International Inc., Morristown, N.J. under the trademarkCAPRON®.

Exemplary of aliphatic/aromatic polyamides includepoly(tetramethylenediamine-co-isophthalic acid) (nylon 4,I),polyhexamethylene isophthalamide(nylon 6,I), hexamethyleneadipamide/hexamethylene-isophthalamide(nylon 6,6/61), hexamethyleneadipamide/hexamethyleneterephthalamide(nylon 6,6/6T),poly(2,2,2-trimethyl hexamethylene terephthalamide), poly(m-xylyleneadipamide) (MXD6), poly(p-xylylene adipamide), poly(hexamethyleneterephthalamide), poly(dodecamethylene terephthalamide), polyamide6T/6I, polyamide 6/MXDT/I, polyamide MXDI, and the like. Blends of twoor more aliphatic/aromatic polyamides can also be used.Aliphatic/aromatic polyamides can be prepared by known preparativetechniques or can be obtained from commercial sources. Other suitablepolyamides are described in U.S. Pat. Nos. 4,826,955 and 5,541,267.

Suitable polyolefins for use herein include polymers of alpha-olefinmonomers having from about 2 to about 6 carbon atoms and includeshomopolymers, copolymers (including graft copolymers), and terpolymersof alpha-olefins. Illustrative homopolymer examples include ultra lowdensity (ULDPE), low density (LDPE), linear low density (LLDPE),metallocene linear low density polyethylene (m-LLDPE), medium density(MDPE), or high density polyethylene (HDPE); polypropylene;polybutylene; polybutene-1; poly-3-methylbutene-1; poly-pentene-1;poly-4-methylpentene-1; polyisobutylene; polyhexene and combinationsthereof.

Polyolefins such as polyethylenes are commonly differentiated based onthe density which results from their numbers of chain branches per 1,000carbon atoms in the polyethylene main chain in the molecular structure.Branches typically are C₃-C₈ olefins, and which are preferably butene,hexene or octene. For example, HDPE has very low numbers of short chainbranches (less than 20 per 1,000 carbon atoms), resulting in arelatively high density, i.e. density ranges from about 0.94 gm/cc toabout 0.97 gm/cc. LLDPE has more short chain branches, in the range of20 to 60 per 1,000 carbon atoms with a density of about 0.91 to about0.93 gm/cc. LDPE with a density of about 0.91 to about 0.93 gm/cc haslong chain branches (20-40 per 1,000 carbon atoms) instead of shortchain branches in LLDPE and HDPE. ULDPE has a higher concentration ofshort chain branches than LLDPE and HDPE, i.e. in the range of about 80to about 250 per 1,000 carbon atoms and has a density of from about 0.88to about 0.91 gm/cc. Illustrative copolymer and terpolymers includecopolymers and terpolymers of alpha-olefins with other olefins such asethylene-propylene copolymers; ethylene-butene copolymers;ethylene-pentene copolymers; ethylene-hexene copolymers; andethylene-propylene-diene copolymers (EPDM). The term polyolefin as usedherein also includes acrylonitrilebutadiene-styrene (ABS)polymers,copolymers with vinyl acetate, acrylates and methacrylates and the like.Preferred polyolefins are those prepared from alpha-olefins, mostpreferably ethylene polymers, copolymers, and terpolymers. The abovepolyolefins may be obtained by any known process. The polyolefin mayhave a weight average molecular weight of about 1,000 to about1,000,000, and preferably about 10,000 to about 500,000. Preferredpolyolefins are polyethylene, polypropylene, polybutylene andcopolymers, and blends thereof. The most preferred polyolefin ispolyethylene. The most preferred polyethylenes are low densitypolyethylenes.

Coextruded with the support layer is a thin polymeric base layer whichmay be comprised of one or more layers of polymeric materials. It shouldbe understood that the thin base layer is a self supporting film whichis capable of being transferred in whole from one substrate to another.The base layer may comprise polyolefins, polyesters, polyamides,polyurethanes, polycarbonates, thermoplastic elastomers, hightemperature polymers such as polyimides and poly ether-ether ketones,and blends thereof. Suitable polyolefins include those listed above.Preferred polyolefins include polypropylene and low densitypolyethylene. Suitable polyesters include polyethylene terephthalate,polyethylene naphthalate and blends thereof. Suitable high temperaturehomopolymers, copolymers or blends may be laminated to producenon-flammable laminates in a cost effective manner. The most preferredmaterial is linear low density polyethylene.

The wet adhesive lamination method of transferring the base film to afabric is accomplished by applying an adhesive directly onto the baselayer by any appropriate means in the art, such as by coating orcoextrusion and drying in an conventional oven if necessary to removesolvent or water. Any suitable adhesive system may be employed such aschemical cross-linkable, moisture curable, 100% solids, U.V curable,electron beam or pressure sensitive adhesive systems. Preferredadhesives include polyurethanes, epoxies, polyesters, acrylics,anhydride modified polyolefin and blends thereof. Modified polyolefincompositions have at least one functional moiety selected from the groupconsisting of unsaturated polycarboxylic acids and anhydrides thereof.Such unsaturated carboxylic acid and anhydrides include maleic acid andanhydride, fumaric acid and anhydride, crotonic acid and anhydride,citraconic acid and anhydride, itaconic acid an anhydride and the like.The adhesive layer may also optionally comprise a colorant, anultraviolet light absorber or both.

In the preferred embodiment of the invention, the fabric may compriseeither a woven or a non-woven fabric suitable for forming the productdesired by the manufacturer. For example, the process of the inventionmay be used in the manufacture of window shades, wherein the fabricpreferably comprises a material suitable for forming window shades.

The support layer and thin base film are preferably attached bycoextrusion. For example, the polymeric material for the individuallayers, are fed into infeed hoppers of a like number of extruders, eachextruder handling the material for one or more of the layers. The meltedand plasticated streams from the individual extruders are fed into asingle manifold co-extrusion die. While in the die, the layers arejuxtaposed and combined, then emerge from the die as a single multiplelayer film of polymeric material. After exiting the die, the film iscast onto a first controlled temperature casting roll, passes around thefirst roll, and then onto a second controlled temperature roll, which isnormally cooler than the first roll. The controlled temperature rollslargely control the rate of cooling of the film after it exits the die.Additional rolls may be employed. In another method, the film formingapparatus may be one which is referred to in the art as a blown filmapparatus and includes a multi-manifold circular die head for bubbleblown film through which the plasticized film composition is forced andformed into a film bubble which may ultimately be collapsed and formedinto a film. Processes of coextrusion to form film and sheet laminatesare generally known. Typical coextrusion techniques are described inU.S. Pat. Nos. 5,139,878 and 4,677,017.

One advantage of coextruded films is the formation of a multilayer filmin a one process step by combining molten layers of each of the supportand base layers, as well as any other optional film layers, into aunitary film structure. The materials of the support and base layers arechosen so that there is a weak cohesive bond strength between thelayers, such that they can be subsequently separated without damage tothe layers. The lamination-delamination process of the present inventionallows relatively thin base films to be applied onto fabrics asdescribed above.

The thin base layer is attached to the fabric by lamination. Laminationtechniques are well known in the art. Typically, laminating is done bypositioning the individual layers on one another under conditions ofsufficient heat and pressure to cause the layers to combine into aunitary structure. In particular, a structure is formed which comprisesthe support layer, a thin base layer on a surface of the support layer,an adhesive layer on the thin base layer, and a fabric on the adhesivelayer. This structure is then passed through the nip of a pair of heatedlaminating rollers by techniques well known in the art. Laminationheating may be done at temperatures ranging from about 50° C. to about175° C., preferably from about 60° C. to about 100° C., at pressuresranging from about 0.034 MPa to about 0.69 MPa, for from about 5 secondsto about 5 minutes, preferably from about less than 1 second to about 1minute.

After the support layer/base layer/adhesive structure is laminated tothe fabric, the support layer is separated from the base layer bydelamination, or by pulling the support layer and the fabric apart,using techniques that are well known in the art. This delamination stepleaves the base layer on the fabric. In order for the base layer toremain on the fabric, the adhesive bond strength between the base layerand the fabric is stronger than the interlayer bond strength between thebase layer and the support layer. In particular, the adhesive bondstrength between the base layer and the fabric is at least 3 times theinterlayer bond strength between the base layer and the support layer;more preferably the interlayer bond strength between the base layer andthe support layer is less than about 35 g/cm, while the adhesive bondstrength between the base layer and the fabric is preferably greaterthan about 200 g/cm, and more preferably greater than about 90 200 g/cm.Therefore, upon pulling the fabric and the support layer apart, the bondbetween the base layer and the support layer will break, leaving thebase layer on the fabric.

Each of the support layer, base layer and adhesive layer may optionallyalso include one or more conventional additives whose uses are wellknown to those skilled in the art. The use of such additives may bedesirable in enhancing the processing of the compositions as well asimproving the products or articles formed therefrom. Examples of suchinclude: oxidative and thermal stabilizers, lubricants, release agents,flame-retarding agents, oxidation inhibitors, oxidation scavengers,dyes, pigments and other coloring agents, ultraviolet light absorbersand stabilizers, organic or inorganic fillers including particulate andfibrous fillers, reinforcing agents, nucleators, plasticizers, as wellas other conventional additives known to the art. Such may be used inamounts, for example, of up to about 10% by weight of the overall layercomposition.

The combination of the base layer and support layer may be orientedprior to being attached to the fabric. The layers may be drawn to drawratios typically used in the art, such as draw ratio of from 1.5:1 to5:1 uniaxially in at least one direction or biaxially in each of itslongitudinal and transverse directions.

Although each layer of the multilayer film structure may have adifferent thickness, the support layer has a preferred thickness of fromabout 10 μm to about 80 μm, more preferably from about 15 μm to about 65μm and most preferably from about 25 μm to about 50 μm. The thin baselayer has a preferred thickness of from about 1 μm to about 10 μm, morepreferably from about 3 μm to about 8 μm and most preferably from about4 μm to about 7 μm. The adhesive layer has a preferred thickness of fromabout 1 μm to about 25 μm, preferably from about 3 μm to about 8 μm, andmore preferably from about 4 μm to about 6 μm. The thickness of thefabric receiver sheet may vary depending upon the desired applicationfor the film of the invention. While such thicknesses are preferred, itis to be understood that other film thicknesses may be produced tosatisfy a particular need and yet fall within the scope of the presentinvention.

The films of the invention are useful for a variety of end applications,such as for forming window shades, upholstery and other uses. The filmsare especially useful in producing fabric laminates which do not allowlight to pass through them, referred to as room darkening. The films ofinvention are also useful for further processing steps prior tolamination such as vacuum metallizing. The process of the inventionenables thinner base films of over 90 inches (2.3 m) wide to belaminated to wider sheets of fabric than are available using techniquescommonly known in the art. Therefore, the utility of such laminates aregreatly expanded over other known laminates, with a softer feel to thefabric and at a reduced cost.

It is also within the scope of the invention that a thin base film maybe attached on both opposing surfaces of the support layer. In thisembodiment, the same steps as described above would be repeated with thesecond base layer being adhesively laminated to a second fabric receiversheet, followed by delamination of said support layer.

The following non-limiting examples serve to illustrate the invention.

EXAMPLE 1

A two layer coextruded film of low density polyethylene and polyamide 6are produced with a polyamide layer thickness of approximately 7 μm anda polyethylene layer of approximately 50 μm. The polyethylene layer isin contact with the chilled casting roll. After casting of thecoextruded film the polyamide surface is corona treated to a surfaceenergy level of greater than 50 dynes. Both layers include a silicaantiblock to prevent blocking during unrolling.

The coextruded film is then metallized on the polyamide surface via avacuum metallization process to deposit aluminum. The amount ofdeposited aluminum is controlled to produce a film with an opticaldensity of greater than 1.5, as required to create a room darkening orblackout effect in the final laminate.

The metallized side of the coextruded film has a two-parts urethaneadhesive applied via a roto-gravure coating process on a Faustelcoater/laminator machine. The adhesive is an epoxy/amine orpolyol/isocyanate urethane coated at a coat weight of 6.5 g/m². Theadhesive is dried in a conventional forced air tunnel at 70° C. fortwenty seconds and then directly laminated to a non-woven fabric using aroom temperature combining nipset with sufficient pressure to adhere themetallized coextruded film to the fabric. The subsequent lamination isthen wound onto a core.

The laminate is allowed to cure for 24 hours after which the aluminumcoated nylon thin film is separated from the supporting polyethylenefilm with a slitting machine. Both the thin film laminated fabric andthe monolayer polyethylene film are simultaneously wound onto separatecores.

The thin film laminated fabric has the same hand and drape as theunlaminated, or receiver, fabric. The thin film-fabric laminate does notallow for the passage of an appreciable amount of light and is roomdarkening in nature.

EXAMPLE 2

Example 1 is repeated except that there is produced a polyethylene layerthickness of approximately 7 μm and a polyamide layer of approximately50 μm by coextrusion with the polyamide layer in contact with thechilled casting roll. After casting, the polyethylene surface is coronatreated to a surface energy level of greater than 50 dynes.

The polyethylene surface is metallized as in Example 1 and thecoextruded film is laminated to a non-woven fabric as in Example 1, withthe adhesive between the polyethylene layer and the fabric. via a vacuummetallization process to deposit aluminum on the thin film side.

After curing for 24 hours, the aluminum coated polyethylene thin film isseparated from the supporting polyamide film with a slitting machine,with both the thin film laminated fabric and the plain polyamide filmbeing simultaneously wound onto separate cores. Similar results areachieved.

EXAMPLE 3

Example 1 is repeated except that the polyamide layer includes TiO₂pigment which is added as a masterbatch at about 5% to produce a whitefilm.

Similar results are achieved, and the white pigmentation of thepolyamide layer results in a laminate with a dull surface.

EXAMPLE 4

Example 2 is repeated, except that a TiO₂ masterbatch is added to thepolyethylene. Similar results are noted, and the white pigmentation ofthe polyamide layer results in a laminate with a dull surface.

It can be seen that the present invention provides a process forobtaining a thin film of a plastic on a fabric in a simple andcost-effective manner.

1. A thin film lamination-delamination process comprising the steps of:a) providing a plastic support layer having first and second surfaces;b) applying at least one thin plastic base layer, having first andsecond surfaces, onto at least one surface of said support layer, withthe first surface of said at least one thin base layer in contact with asurface of said support layer; c) applying an adhesive layer onto thesecond surface of said second base layer; d) attaching the base layer toa fabric via the adhesive layer; and e) separating the support layerfrom the base layer, such that the base layer remains attached to thefabric.
 2. The process of claim 1 further comprising conducting steps b)through e) on the second surface of said support layer.
 3. The processof claim 1 wherein the adhesive bond strength between said base layerand said fabric is at least 3 times the interlayer bond strength betweensaid base layer and said support layer.
 4. The process of claim 1wherein the interlayer bond strength between said base layer and saidsupport layer is about 35 g/cm or less.
 4. The process of claim 1wherein said support layer comprises a material selected from the groupconsisting of polyolefins, polyamides, polyesters, polyvinyl chloride,ethylene vinyl acetate, cyclo olefin polymers, and blends thereof. 5.The process of claim 1 wherein said base layer comprises a polyethylene.6. The process of claim 1 wherein said base layer comprises a polyamide.7. The process of claim 1 wherein said base layer comprises a materialselected from the group consisting of polyolefins, polyesters,polyamides, polyurethanes, polycarbonates, thermoplastic elastomers,high temperature polymers, and blends thereof.
 8. The process of claim 1further comprising metallizing said second surface of said base layerprior to applying said adhesive.
 9. The process of claim 1 wherein saidadhesive layer comprises a material selected from the group consistingof polyurethanes, epoxies, polyesters, acrylics, anhydride modifiedpolyolefin and blends thereof.
 10. The process of claim 1 wherein saidfabric comprises a non-woven fabric.
 11. The process of claim 1 whereinsaid base layer has a thickness of from about 1 μm to about 10 μm andsaid support layer has a thickness of from about 25 μm to about 50 μm.12. The process of claim 1 wherein said base layer has a thickness offrom about 4 μm to about 7 μm.
 13. The process of claim 1 wherein saidbase layer is applied to said support layer by coextrusion.
 14. Amultilayered film comprising: a) a plastic support layer having firstand second surfaces; b) at least one thin plastic base layer, havingfirst and second surfaces, on at least one of said surfaces of saidsupport layer, with the first surface of said at least one thin baselayer in contact with a surface of said support layer; c) an adhesivelayer on said second surface of said thin base layer; and d) a fabricattached to said thin base layer via said adhesive layer.
 15. Themultilayered film of claim 14 further comprising an additional thin baselayer on the second surface of the support layer, and an additionalfabric attached to the second surface of the support layer via a secondadhesive layer.
 16. The multilayered film of claim 14 wherein theadhesive bond strength between said base layer and said fabric is atleast 3 times the interlayer bond strength between said base layer andsaid support layer.
 17. The multilayered film of claim 16 wherein theinterlayer bond strength between said base layer and said support layeris about 35 g/cm or less.
 18. The multilayered film of claim 14 whereinsaid support layer comprises a material selected from the groupconsisting of polyolefins, polyamides, polyesters, polyvinyl chloride,ethylene vinyl acetate, cyclo olefin polymers, and blends thereof. 19.The multilayered film of claim 14 wherein said base layer comprises amaterial selected from the group consisting of polyolefins, polyesters,polyamides, polyurethanes, polycarbonates, thermoplastic elastomers,high temperature polymers, and blends thereof
 20. The multilayered filmof claim 19 wherein said base layer comprises a polyethylene.
 21. Themultilayered film of claim 14 wherein said base layer has a metallizedsurface.
 22. The multilayered film of claim 14 wherein said adhesivelayer comprises a material selected from the group consisting ofpolyurethanes, epoxies, polyesters, acrylics, anhydride modifiedpolyolefin and blends thereof.
 23. The multilayered film of claim 14wherein said fabric comprises a non-woven fabric.
 24. The multilayeredfilm of claim 14 wherein said base layer has a thickness of from about 1μm to about 10 μm and said support layer has a thickness of from about10 μm to about 80 μm.
 25. The multilayered film of claim 14 wherein saidbase layer has a thickness of from about 4 μm to about 7 μm.
 26. Amultilayered film comprising: a) a fabric having a surface; and b) athin plastic base layer attached to the surface of said fabric; whereinsaid base layer has a thickness of from about 1 μm to about 10 μm, andwherein said thin base layer is adhesively attached to the fabric.
 27. Amultilayered film produced by the process of claim 1.